Senior Oncology Clinical Development Leader

AbbVie; San Francisco (CA); On-site; USD 180,000 - 240,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Job summary

AbbVie is seeking an experienced leader to oversee direction, planning and interpretation of clinical trials within one or more development programs. You will lead cross-functional teams to generate high-quality data that informs product strategy and regulatory submissions.

The role requires extensive clinical trial experience, leadership across global teams, and strong knowledge of regulatory requirements and GCP standards. Excellent communication in English is essential.

Qualifications

• Bachelor's degree in the sciences; advanced degree preferred.
• 8+ years of relevant clinical trial experience.
• Ability to run a complex clinical research program independently.
• Proven leadership and cross-functional collaboration skills.
• Excellent oral and written English communication.
• Extensive knowledge of clinical trial methodology and regulatory requirements.

Responsibilities

• Leads and ownership of multiple clinical development programs in support of the plan.
• Oversees education of investigators, site personnel and AbbVie study staff.
• May lead clinical study teams and monitor study integrity and data.
• Owns design, analysis, interpretation and reporting of protocols and study reports.
• Oversees senior scientists and may supervise direct reports.
• Participates in Integrated Evidence Strategy Teams to develop a Clinical Development Plan.
• Acts as in-house clinical expert coordinating with internal stakeholders.
• Keeps up with regulatory and compliance requirements for trials.
• Ensures adherence to Good Clinical Practices and pharmacovigilance standards.

Skills

Leadership

Communication

Cross-functional collaboration

Regulatory knowledge

Project management

Education

Bachelor's degree in sciences

MS/PhD preferred

Job description

AbbVie is seeking an experienced leader to oversee direction, planning and interpretation of clinical trials within one or more development programs. You will lead cross-functional teams to generate high-quality data that informs product strategy and regulatory submissions.

The role requires extensive clinical trial experience, leadership across global teams, and strong knowledge of regulatory requirements and GCP standards. Excellent communication in English is essential.